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Tecomet RC302002-J

by Tecomet, Inc

Tecomet RC302002-J is a Class I device made by Tecomet, Inc, listed in FDA GUDID since 8 Oct 2020 (UDI-DI 00818069018092), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00818069018092 UDI-DI Date8 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Tecomet
Generic name
Orthopaedic implantable-device cutter
Model / reference
RC302002-J
Primary DI / UDI-DI
00818069018092
FDA product code
FZT
GMDN term
Orthopaedic implantable-device cutter
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implantable-device cutter

Similar devices in this category

Other devices filed under Orthopaedic implantable-device cutter.

Other devices from Tecomet, Inc

See all devices from Tecomet, Inc →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)